Mitral valve annuloplasty ring

ABSTRACT

A mitral valve annuloplasty ring and method for implanting a mitral valve annuloplasty ring to treat mitral insufficiency by reestablishing the normal shape and contour of the mitral valve annulus. The annuloplasty ring is flexible and can be readily adjusted to different sizes and shapes. The method substantially eliminates scarring subsequent to the annuloplasty procedure to maintain flexibility of the ring and the annulus indefinitely.

BACKGROUND

[0001] The present invention is directed to a mitral valve annuloplastyring and a method for implanting a mitral valve annuloplasty ring totreat mitral insufficiency in a patient. Mitral insufficiency, alsoknown as mitral regurgitation, is a common cardiac abnormality whereinthe heart's mitral valve does not properly close.

[0002] In a normally functioning heart, oxygenated blood passes from theleft atrium through the opened mitral valve and into the left ventriclewhen the left ventricle is in a relaxed state. When the left ventriclecontracts, the blood is pushed out of the left ventricle thereby closingthe mitral valve to prevent blood flowing back or regurgitating into theleft atrium. From the left ventricle, the oxygenated blood is pumped outof the heart and directed to the rest of the body.

[0003] With mitral insufficiency, the mitral valve does not fully closeand a portion of blood leaks back into the left atrium when the leftventricle contracts. As a result, the heart has to work harder bypumping not only its regular volume of blood, but also the extra volumeof blood that regurgitates back into the left atrium. The added workloadcreates an undue strain on the left ventricle. This strain caneventually wear out the heart and result in death when the condition isprolonged and severe enough. Consequently, a properly functioning mitralvalve is critical to the pumping efficiency of the heart.

[0004] Mitral valve annuloplasty is a well known approach for treatingmitral insufficiency, although other treatments are used which includereplacing the mitral valve, repairing the mitral valve leaflets, andshortening or replacing the chordae tendinae. Mitral valve annuloplastyis the reparation of the mitral valve annulus which effects full closureof the leaflets by reestablishing the size and shape of the normalmitral valve annulus. Such an annuloplasty most commonly incorporatesthe use of a mitral annuloplasty ring wherein the ring is implanted onthe mitral valve annulus.

[0005] There are three basic types of mitral annuloplasty rings used inannuloplasty procedures. They include a rigid ring, a flexible ring anda combined ring that has both a flexible component and a rigidcomponent.

[0006] Due to their inflexibility, the rigid rings dictate the shape andcontour of the mitral valve. The native mitral valve annulus flexes inresponse to the movement of the heart. However, with a rigid ring theannulus is not able to flex normally or move freely with the pumpingaction of the heart. As a result of the rigidity, the physiologicfactors that normally shape the mitral valve annulus are not allowed totake precedence in shaping the valve.

[0007] Another drawback with rigid rings is that they can induce a heartcondition known as systolic anterior motion in patients having a mitralvalve posterior leaflet that is too “tall”. During ventricularcontraction, the posterior leaflet pushes the anterior leaflet in adirection opposite to the anterior leaflet's normal movement, resultingin the obstruction of the left ventricle's outflow tract.

[0008] Overall, rigid annuloplasty rings do not allow the mitral valveannulus to reestablish its normal shape and form as dictated by theaction of the heart pumping. The shape and contour of the annulus isestablished by the inflexible shape and form of the ring itself.

[0009] Flexible rings made of Dacron cloth, unlike the rigid rings, canallow the mitral valve annulus to move and flex as the heart contractsand relaxes. However, several drawbacks still exist. Proper shape andcontour of the annulus is necessary in order for the mitral valveleaflets to close effectively. One shortcoming of the flexible ring isits predisposition to crimp during implantation. Crimping can bedetrimental to the valve annulus, sometimes resulting in a mitralorifice that is too small. This can lead to stenosis of the valve.Furthermore, neither the flexible rings nor the combined rings willremain flexible indefinitely after annuloplasty. Since the rings aresecured in place by a line of sutures attached directly to the annulus,scarring and resultant stiffening of the annulus inevitably develops.This loss of flexibility impedes the normal flexing and movement of theheart, particularly the left ventricle and, therefore, the heart cannotfunction optimally.

SUMMARY

[0010] The annuloplasty ring of the present invention is a combined ringwhich comprises a first section that is substantially rigid and a secondflexible section. The ring can be readily adjusted to fit the annulus ofany particular patient. The method of implanting the annuloplasty ringof the present invention comprises installing a ring within the fat padof the atrioventricular groove which surrounds the mitral valve annulus.The method does not require a series of sutures extending through themitral valve annulus tissue to hold the ring in place. Resultantscarring and stiffening of the annulus is thereby substantiallyeliminated.

[0011] The ring of the present invention when combined with the methodof the present invention is positioned in the fat pad of theatrioventricular groove adjacent to the mitral valve annulus. Theflexible section of the ring extends adjacent to the flexible posteriorportion of the annulus, while the rigid section of the ring spans thesubstantially rigid inter-trigone section of the annulus. Since theflexible section of the ring is held in the atrioventricular groove ofthe posterior section of the annulus, it is not necessary to suture theflexible section directly to the mitral valve annulus. As a result,scarring of the annulus is substantially eliminated, thereby allowingthe ring and annulus to remain flexible indefinitely. As in the normalheart, this flexibility enables the mitral valve annulus to flex inseveral planes during contraction and relaxation of the heart. Theresult is better postoperative functioning of the mitral valve andbetter postoperative functioning of the left ventricle, as well.

[0012] It is an object of the present invention to provide anannuloplasty ring that reestablishes the normal shape and contour of themitral valve annulus.

[0013] It is a further object of the present invention to provide amethod for performing an annuloplasty that substantially eliminatesscarring of the mitral valve annulus tissue to preclude the loss offlexibility following the annuloplasty.

[0014] It is a further object of the present invention to provide amethod for implanting the annuloplasty ring that allows the ring tomaintain flexibility indefinitely.

[0015] It is a further object of the invention to provide anannuloplasty ring that is flexible enough to allow the mitral valve andannulus to flex through different planes, yet positioned such that theshape and contour of a normal mitral valve annulus is reestablished.

[0016] It is a further object of the present invention to provide aflexible annuloplasty ring that does not crimp during implantation.

[0017] It is a further object of the present invention to provide anannuloplasty ring that can be flexed in all manner that the nativemitral valve annulus flexes.

[0018] It is a further object of the present invention to provide anannuloplasty ring and method of implanting the ring that maintainsflexibility of the ring and the mitral valve annulus indefinitely.

[0019] It is a further object of the present invention to provide amethod for implanting the annuloplasty ring that minimizes scarring ofthe mitral valve annulus and nearby tissue.

[0020] It is a further object of the present invention to provide anannuloplasty ring that assumes the shape of the normal mitral valveannulus to allow for effective functioning of the valve.

[0021] It is a further object of the present invention to provide anannuloplasty ring and method of implanting the ring that result ineffective coaptation of the anterior and posterior leaflets of themitral valve.

[0022] It is a further object of the present invention to provide anannuloplasty ring and method of implanting an annuloplasty ring that donot impede the movement of the left ventricle's base when the ventricleis contracting and relaxing, thereby allowing effective functioning ofthe left ventricle.

[0023] It is a further object of the present invention to provide anannuloplasty ring and a method of surgically implanting an annuloplastyring that allow the base of the left ventricle to assume its full rangeof movement when contracting and relaxing to allow effective functioningof the left ventricle.

[0024] It is a further object of the present invention to provide anannuloplasty ring that allows the left ventricle to move naturally asthe heart pumps and allows the mitral valve annulus to flex freely inresponse to the movement of the left ventricle.

[0025] It is a further object of the present invention to provide anannuloplasty ring and a method of implanting the annuloplasty ring thatdoes not require a plurality of sutures along the posterior portion ofthe mitral valve annulus to secure the ring in place.

[0026] It is a further object of the present invention to provide anannuloplasty ring that can be readily adjusted in size.

[0027] It is a further object of the present invention to provide anannuloplasty ring that can be readily adjusted in shape by adjusting thecircumference of the ring.

[0028] It is a further object of the present invention to provide a kitfor an annuloplasty ring that reestablishes the normal shape to andcontour of the mitral valve annulus.

BRIEF DESCRIPTION OF THE DRAWINGS

[0029] FIGS. 1A-1F are cutaway views of the heart as seen from theatrial position depicting a preferred method of implanting the mitralvalve annuloplasty ring in the atrioventricular groove.

[0030]FIG. 2A is a top view of a preferred embodiment of the mitralvalve annuloplasty ring of the present invention in a closedconfiguration.

[0031]FIG. 2B is a side view of the mitral valve annuloplasty ring in aclosed configuration.

[0032]FIG. 3 is an exploded view of the mitral valve annuloplasty ringwith needle.

[0033]FIG. 4 is a schematic cross sectional side view of a portion ofthe heart depicting the atrioventricular groove with the annuloplastyring implanted therein.

[0034]FIG. 5 is a view of the mitral valve annuloplasty ring in asurgical configuration.

[0035]FIG. 6 is a view of the mitral valve annuloplasty ring in an openconfiguration.

DETAILED DESCRIPTION

[0036] The left ventricle is the main pumping chamber of the heart.Oxygenated blood from the lungs enters the left atrium and passes intothe left ventricle through the mitral valve. The blood is pumped fromthe left ventricle to the rest of the body.

[0037] As shown in FIGS. 1A-1F, the mitral valve (30) is a one waypassive valve comprising a pair of leaflets, including a larger anteriorleaflet (32) and a smaller posterior leaflet (33). The leaflets open andclose in response to pressure differences in the heart (5) on eitherside of the mitral valve (30). The base of each anterior (32) andposterior (33) leaflet is attached to the mitral valve annulus (34).

[0038] The contour of the mitral valve annulus (34) refers to theoutline or form of the annulus (34) when viewed in the general plane ofthe annulus (34). The shape of the annulus (34) is that shape viewedfrom the atrial side of the mitral valve (30), “looking down” on themitral valve annulus (34).

[0039] The mitral valve annulus (34) includes a posterior portion (35)and an anterior portion (36). The anterior portion (36), also known asthe inter-trigone segment or section, is a generally straight,substantially rigid segment. The posterior portion (35) of the annulus(34) is a flexible, curvilinear segment that encompasses a largerproportion of the annulus circumference than the anterior portion (36).The right (37) and left (38) fibrous trigones mark the ends of thegenerally straight segment and define the intersection points betweenthe posterior (35) and anterior portions (36).

[0040] Referring to FIGS. 2A and 2B, there is shown a preferredembodiment of the annuloplasty ring (10) comprising the presentinvention. The ring (10) comprises a first section (11) and a secondsection (15). The first section (11) has a first end (12) and a secondend (13), while the second section (15) includes a proximal end (16) anda distal end (17). A means for sizing the annuloplasty ring (10)includes measurement indicia (18) extending inwardly from an outermostedge of the second section's distal end (17). The annuloplasty ring (10)also includes a detachable needle (20) having a tip (72) and anattaching end (73) as shown in FIG. 3.

[0041] The annuloplasty ring (10) comprises a first means for joiningthe second end of the first section to the distal end of the secondsection and a second means for joining the first end of the firstsection to the proximal end of the second section. The ring (10) alsocomprises a third means for joining the second end of the second sectionto the needle.

[0042] In one preferred embodiment, the first means for joining thesecond end of the first section to the distal end of the second section,the second means for joining the first end of the first section to theproximal end of the second section, and the third means for joining thesecond end of the second section to the needle comprise frictionalengagements.

[0043] The frictional engagements include a hollow inner portion (19) inthe second section (15) having exterior openings (71) at the proximal(16) and distal (17) ends. The hollow inner portion (19) can extend theentire length of the second section (15) or alternately, it can belimited to the ends (16, 17) of the second section (15). The hollowportion (19) has an inner diameter that is approximately equal to theouter diameter of the first (12) and second (13) ends of the firstsection (11) and also that is approximately equal to the outer diameterof the attaching end (73) of the needle (20).

[0044] The exterior openings (71) of the hollow inner portion (19) onthe proximal end (16) of the second section (15) receives the first end(12) therein, while the exterior opening (71) of the hollow innerportion (19) on the distal end (17) receives the second end (13) of thefirst section and, alternately, the attaching end (73) of the needle(20). When the ends (12, 13) of the first section (11) are insertedthrough the exterior openings (71) into the hollow inner portion (19), africtional engagement is created between the respective inner and outerdiameters which secures the ends of the sections (11, 15) together.Likewise, when the attaching end (73) of the needle (20) is insertedthrough the exterior opening (71) into the hollow inner portion (19) ofthe distal end (17), the needle (20) is held within the hollow innerportion (19) by frictional engagement.

[0045] Although the first means for joining the second end of the firstsection to the distal end of the second section, the second means forjoining the first end of the first section to the proximal end of thesecond section, and the third means for joining the second end of thesecond section to the needle comprise frictional engagements, anysuitable and separate types of means could be used instead.

[0046] The first (11) and second (15) sections are elongated. In onepreferred embodiment, the first section (11) has a bow or bend (70) inthe center region. The bow (70) is offset approximately 1.0 mm from areference plane in which the first (12) and second (13) ends arelocated. In another preferred embodiment, the first section of the ringis straight and does not have a bow.

[0047] The first section (11) is made from a substantially rigidmaterial. It is preferable that the material is able to maintain itsrigidity indefinitely and also preferable that it is inert or compatiblewith body tissues. Examples of materials that could be used for thefirst section (11) are titanium, stainless steel, pyrolytic carbon andvarious plastics. Also, other suitable materials of choice could beused, as well.

[0048] The material comprising the second section (15) is flexible andis capability of being affixed to the first section. Preferably, thematerial is inert or compatible with body tissues. Examples of materialsthat could be used for the second section include silastic,polyethylene, Dacron and Teflon. Also, other suitable materials ofchoice could be used, as well.

[0049] The annuloplasty ring (10) of the present invention reestablishesthe normal shape and contour to the mitral valve annulus (34). The firstsection (11) of the annuloplasty ring (10) is adjacent to theinter-trigone section (36) after implantation, as shown in FIGS. 1A-1F.The curvature of the bow (70) is oriented to conform to the portion ofthe mitral valve annulus (34) that is located adjacent to the aorticvalve root. Both the first section (11) and the inter-trigone section(36) are substantially rigid. Since the inter-trigone section (36) doesnot normally bend in response to the movements of the heart, it is,therefore, not required for the first section (11) to bend or flexeither.

[0050] The second section (15) is implanted adjacent to the posteriorportion (35) of the annulus. Both the posterior portion (35) and thesecond section (15) are flexible and, as a result, can flex and movewith the natural movements of the heart, as the left ventricle relaxesand contracts. Furthermore, the method of implanting the annuloplastyring within the fat pad (40) of the atrioventricular groove (39), asshown in FIG. 4, ensures that the annulus and the second section (15) ofthe ring (10) will remain flexible indefinitely.

[0051] Referring again to FIGS. 1A-1F, the needle (20) acts as a leaderguide to implant the ring (10) in the proper location and position inthe atrioventricular groove (39) around the mitral valve annulus (34).The tip (72) of the needle is preferably a round-tip which is sharpenough to penetrate the tissue for implantation, yet blunt enough tomaneuver within the atrioventricular groove without damaging criticalareas.

[0052] The size and shape of the annuloplasty ring (10) can be adjusted.Using the measurement indicia (18) on the second section (15) as aguide, the appropriate length of the section is established, then anyunnecessary length on the second section (15) can be removed by cutting,as shown in FIG. 1D. By changing the length of the second section (15),the circumference of the annuloplasty ring is also changed.

[0053] As shown in FIG. 2A, the second means for joining the first endof the first section to the proximal end of the second section and thefirst means for joining the second end of the first section to thedistal end of the second section secures the ends (12, 13) of the firstsection (11) to the respective ends (16, 17) of the second section (15)to form a closed loop. In one preferred embodiment in which the firstand second means for joining comprise frictional engagements, theproximal (16) and distal (17) ends of the second section are preferablydisposed adjacent to each other at a center region of the first section(11), thereby covering a substantial portion of the first section (11).Alternately, the second end (13) of the first section (11) can be freeand unattached while the distal end (17) of the second section (15) isattached to the needle (20) for performing the annuloplasty as shown inFIG. 5.

[0054] The length of the first section (11) is shorter than the lengthof the second section (15). The length of first section (11) can vary,but it is preferred that its length be no more than about 50-75% of thelength of the inter-trigone section (36) of the mitral valve annulusbeing repaired. The requisite proportion for a particular annuloplastyring will depend on the flexibility of the second section (15). As forexample, the more flexible the material forming the second section (15),the longer the length of the first section (11) should be relative tothe length of the inter-trigone section (36). Conversely, the lessflexible the material of the second section (15), the shorter therelative length of the first section (11) should be relative to thelength of the inter-trigone portion (36).

[0055] The lengths of the two sections can be varied relative to eachother in order to achieve various shapes for the closed loop of theannuloplasty ring (10). For example, by lengthening the first section(11) relative to the length of the second section (15), the annuloplastyring will become “flatter” as characterized by a smaller anterior toposterior distance.

[0056] In one preferred embodiment of the present invention, the firstsection (11) has a length of approximately 1.5 cm and an overalldiameter of approximately 6 mm. The diameter can, however, vary so longas it fits the mitral valve annulus under repair and it precludesinadvertent deformation or breakage of the ring.

[0057] In one preferred embodiment, the indicia (18) are markings spacedat intervals of about 1.0 mm. However, the intervals could be spaced atany desired distance, extending for any desired length along the secondsection (15).

[0058] An open configuration of the annuloplasty ring (10) is shown inFIG. 6 wherein the first section (11) has its first end (12) attached tothe second section's proximal end (16). The second end (13) of the firstsection (11) and the distal end (17) of the second section (15) areunattached.

[0059] A closed configuration, shown in FIG. 2A, comprises the first end(12) of the first section (11) being attached to the proximal end (16)of the second section (15) and the second end (13) of the first section(11) being attached to the distal end (17) of the second section (15).In the closed configuration, the annuloplasty ring (10) forms the closedloop. After the annuloplasty procedure, the ring (10) is in its closedconfiguration.

[0060] In FIG. 5, the annuloplasty ring (10) of the present invention isshown in a surgical configuration in which the first end (12) of thefirst section (11) is attached to the proximal end (16) of the secondsection (15) and the needle (20) is attached to the distal end (17) ofthe second section (15). The second end (13) of the first section (11)is unattached. The surgical configuration is designated primarily foruse during the annuloplasty procedure.

[0061] After the annuloplasty ring (10) is implanted as in FIG. 1E, thefirst section (11) is in alignment with the inter-trigone section (36)of the mitral valve annulus (34) such that the bow (70) conforms to thecontour of the annulus (34) adjacent to the aortic valve root. Theinter-trigone section (36) which extends between the left (38) and right(37) fibrous trigones is substantially rigid, as is the first section(11) of the ring. The second section (15) is primarily implanted aroundthe posterior portion (35) of the annulus (34) and within the fat pad(40) of the atrioventricular groove (39) as shown in FIG. 4. Along withthe posterior portion (35) of the annulus (34), the second section (15)is allowed to move and flex freely with the movements of the heart.

[0062] Referring to FIGS. 1A-1E, the annuloplasty ring (10) is installedadjacent to the mitral valve annulus (34) and within the fat pad (40) ofthe atrioventricular groove (39). After the ring (10) is implanted, thesecond section (15) is cut to the appropriate size for the patient. Thedistal end (17) of the second section (15) is then attached to the firstsection (11). Preferably, the ring (10) is sutured to the annulus at theleft and right fibrous trigones. However, this suturing may be avoidedif deemed not necessary.

[0063] To implant the annuloplasty ring in a patient, the needle (20) isattached to the distal end (17) of the second section (15) and the firstend (12) of the first section (11) is attached to the proximal end (16)of the second section (15), as shown in the surgical configuration ofFIG. 5. In one preferred embodiment, the needle is attached by insertingits attaching end (73) into the exterior opening (71) of the hollowinner portion (19) of the second section (15).

[0064] The tip of the needle (20) is passed through the endocardium (65)and the left atrial myocardial wall (46) from the endocardial aspect atthe right fibrous trigone (37), as shown in FIG. 1A, simultaneouslypulling the first (11) and second (15) sections of the ring (10) behindit, such that a portion of the second section (15) eventually passesthrough the left atrial myocardial wall (46) as in FIG. 1B. The needle(20) is passed in a posterior direction just external to and parallel tothe mitral valve annulus (34). The tip of the needle (20) is passedaround the outside curvature of the mitral valve annulus (34) and withinthe fat pad (40) of the atrioventricular groove (39). The needle (20) ismoved in a clockwise direction towards the left fibrous trigone (38).

[0065] At the left fibrous trigone (38), the needle's tip (72) is passedback through the left atrial myocardial wall (46) from the epicardium(60) and back through the endocardium (65) at the left fibrous trigone(38), thereby pulling the first section (11) into position along theanterior portion (36) and pulling the second section (15) into positionwithin the atrioventricular groove (39) such that the second section(15) is adjacent to the posterior portion (35) of the mitral valveannulus (34), as shown in FIG. 1C.

[0066] Referring to FIG. 1D, the annuloplasty ring (10) is sized usingthe measurement indicia (18) to determine the appropriate length of thesecond section (15) and hence the appropriate circumference for theannuloplasty ring (10). The distal end (17) can be cut to size, ifrequired, by severing the second section (15) at a selected location onthe second section (15). The needle (10) can be removed prior to sizingand/or cutting of the second section (15) or, alternately, it can remainattached to the ring (10) during sizing and/or cutting.

[0067] The distal end (17) of the second section (15) is then joined tothe second end (13) of the first section (11). In one preferredembodiment as shown in FIG. 1E, the second end (13) and distal end (17)are joined by frictional engagement wherein the second end (13) of thefirst section (11) is inserted into the hollow inner portion (19) of thesecond section, until the distal (17) and proximal (16) ends of thesecond section (15) approach one another approximate a center point onthe first section (11).

[0068] In another embodiment of the method for implanting theannuloplasty ring, the procedure is reversed in direction, wherein thetip (72) of the needle (20) is first passed through the endocardium (65)and the left atrial myocardial wall (46) from the endocardial aspect atthe left fibrous trigone (38) and passed in a posterior directionsubstantially parallel to the annulus (34). The needle (20) is moved ina counterclockwise direction around the annulus (34) to the rightfibrous trigone (37). Here, at the right fibrous trigone (37), theneedle's tip (72) is passed back through the left atrial myocardial wall(46) from epicardium (60) and back through the endocardium (65). Theprocedure then continues as the above procedure is performed in theopposite, counterclockwise direction.

[0069] After the annuloplasty ring is in place sutures (80, 81) shown inFIG. 1F can be added to secure the annuloplasty ring to the annulus. Aplurality of sutures (80) can be used to fix the ring (10) to theinter-trigone section (36), preferably at the left and right fibroustrigones. Since the inter-trigone section (36) is substantially rigid inthe native mitral valve annulus, any scarring that may result from thesesutures (80) would not substantially interfere with the normal flexingof the rest of the annulus and movement of the left ventricle.

[0070] In addition, at least one suture (81) may be used to fix thesecond section (15) within the atrioventricular groove (39) as an addedprecaution for guarding against possible slippage of the ring (10) afterit is implanted. This suture (81) would preferably be located near themidpoint of the second section (15).

[0071] The preferred embodiments of the present invention allow themitral valve annulus to maintain its normal flexure, which in turnenables the left ventricle to move in a normal manner as it contractsand relaxes. Furthermore, the method of implanting allows theannuloplasty ring and the annulus, as well, to maintain flexibilityindefinitely after the annuloplasty, since it is not necessary to securethe ring in place with a line of sutures through the mitral valveannulus tissue of the posterior portion.

[0072] The ring further reestablishes the normal shape and contour ofthe mitral valve annulus which allows for effective coaptation of theanterior and posterior leaflets of the valve. Additionally, the size andshape of the ring can be adjusted making it easily adaptable todifferent patients.

[0073] In one example, the annuloplasty ring of the present inventioncan be manufactured using a flexible material that is also elastic tocomprise the second section. The elasticity of the ring wouldaccommodate the expansion of the mitral annulus during relaxation of theleft ventricle and accommodate contraction of the annulus duringcontraction of the left ventricle. In other words, the annulus wouldexpand and contract, in addition to flexing, with the expansion andcontraction of the left ventricle.

[0074] In another example, the first (11) and second (15) sections arejoined integrally at the respective first (12) and proximal (16) ends,wherein the first section remains substantially rigid and the secondsection (15) remains flexible. The integral joining of the two sectionscan be done by coextrusion, molding or other suitable manufacturingtechniques of choice.

[0075] Although the present invention has been described in considerabledetail with reference to certain preferred versions thereof, otherversions are possible. Therefore, the spirit and scope of the appendedclaims should not be limited to the description of the preferredversions contained herein.

1. An annuloplasty ring for repairing a valve in a patient's heart, saidannuloplasty ring comprising: (a) a first section for implantingadjacent to the valve; and (b) a second flexible section for implantingwithin a fat pad of an atrioventricular groove in the heart.
 2. Theannuloplasty ring of claim 1, wherein said second flexible sectioncomprises a proximal end and a distal end and a means for joining thedistal end to a needle.
 3. The annuloplasty ring of claim 2, furthercomprising a needle having an attaching end with an outer diameter. 4.The annuloplasty ring of claim 3, wherein said means for joining thedistal end to the needle comprising a frictional engagement.
 5. Theannuloplasty ring of claim 4, wherein said first section furthercomprises a first and second end, said first and second ends having anouter diameter; said annuloplasty ring further comprising: (a) a firstmeans for joining the distal end of the second flexible section to thesecond end of the first section; and (b) a second means for joining theproximal end of the second flexible section to the first end of thefirst section.
 6. The annuloplasty ring of claim 5, wherein said firstmeans for joining comprises a frictional engagement and said secondmeans for joining comprises a frictional engagement.
 7. The annuloplastyring of claim 6, wherein said outer diameters of said first and secondends are approximately equal to said inner diameter of said hollow innerportion, and said frictional engagement of said first means for joiningis between said inner diameter of said hollow inner portion at saiddistal end and said outer diameter of said second end, and saidfrictional engagement of said second means for joining is between saidinner diameter of said hollow inner portion at said proximal end andsaid outer diameter of said first end.
 8. The annuloplasty ring of claim5, further comprising: (a) an open configuration wherein said firstsection is attached to said second section by said second means forjoining and said second end of said first section and said distal end ofsaid second flexible section are unattached; (b) a closed configurationwherein said first section is attached to said second section by saidfirst and second means for joining, thereby forming a loop; and (c) asurgical configuration wherein said first section is attached to saidsecond section by said first means for joining and said second flexiblesection is attached to the needle by said means for joining said distalend of said second flexible section to said needle.
 9. The annuloplastyring of claim 4, wherein the distal end of the flexible section furthercomprises a hollow inner portion with an inner diameter approximatelyequal to the outer diameter of the attaching end of the needle and saidfrictional engagement is between said inner diameter and said outerdiameter of the attaching end.
 10. The annuloplasty ring of claim 1,wherein said first section is rigid with first and second ends beingsubstantially straight, said first section further having a bow betweenthe first and second ends.
 11. The annuloplasty ring of claim 1, furthercomprising a means for sizing the ring.
 12. A method for implanting anannuloplasty ring in a patient's heart, comprising: implanting aflexible section of the annuloplasty ring in the fat pad of theatrioventricular groove of the heart; positioning a rigid section of theannuloplasty ring adjacent to the valve annulus; and forming theannuloplasty ring into a closed loop.
 13. The method of claim 12,wherein the annuloplasty ring includes a needle attached to the flexiblesection.
 14. The method of claim 13, wherein the steps of implanting asubstantial portion of the annuloplasty ring in the fat pad of theatrioventricular groove further comprises: inserting the tip of theneedle through the endocardium and the left atrial myocardial wall fromthe endocardial aspect at the right fibrous trigone; passing the needleand a portion of the annuloplasty ring through the endocardium and theleft atrial myocardial wall from the endocardial aspect, at the rightfibrous trigone; passing the needle and a portion of the annuloplastyring in a posterior direction, external to and parallel to the mitralvalve annulus; and inserting the tip of the needle through left atrialmyocardial wall from the epicardial aspect and back through theendocardium at the left fibrous trigone; passing the needle and aportion the annuloplasty ring back through the left atrial myocardialwall from the epicardial aspect and back through the endocardium at theleft fibrous trigone.
 15. The method of claim 14, wherein positioningthe rigid n further comprises: positioning the flexible section in asubstantial parallel orientation with the posterior portion of themitral valve annulus, by pulling the needle; aligning the rigid sectionof the annuloplasty ring along an anterior portion of the mitral valveannulus; and positioning the bow of the rigid section to conform with acontour of the mitral valve annulus adjacent the aortic valve root. 16.The method of claim 13, further comprising: determining the appropriatesize of the annuloplasty ring after implanting and positioning the ringand before forming the ring into a closed loop; and cutting theannuloplasty ring to the appropriate size.
 17. The method of claim 16,further comprising: detaching the needle from the annuloplasty ringafter implanting and positioning the ring and before determining theappropriate size.
 18. The method of claim 16, wherein the step offorming the annuloplasty ring into a closed loop further comprises:joining a second end of the rigid section to a distal end of theflexible section by inserting the second end of the rigid section into ahollow inner portion of the distal end of the flexible section.
 19. Themethod of claim 12, further comprising: suturing the annuloplasty ringto the valve annulus at the left and right fibrous trigones.
 20. Themethod of claim 19, further comprising: suturing the annuloplasty ringwithin the fat pad of the atrioventricular groove.
 21. A kit for anannuloplasty ring comprising: (a) a first section; (b) a second flexiblesection having a proximal end and a distal end; (c) a means for joiningthe distal end of the second flexible section to a needle.
 22. The kitfor an annuloplasty ring in claim 21, further comprising a needle havingan attaching end with an outer diameter.
 23. The kit for an annuloplastyring in claim 22, wherein said means for joining the distal end to theneedle comprising a frictional engagement.
 24. The kit for anannuloplasty ring in claim 23, wherein said first section furthercomprises a first end and a second end, said first and second endshaving an outer diameter, and said annuloplasty ring further comprising:(a) a first means for joining the distal end of the second flexiblesection to the second end of the first section; and (b) a second meansfor joining the proximal end of the second flexible section to the firstend of the first section.
 25. The kit for an annuloplasty ring in claim24, wherein said first means for joining comprises a frictionalengagement and said second means for joining comprises a frictionalengagement, said second flexible section includes a hollow inner portionat the distal and proximal ends, said hollow inner portion having aninner diameter approximately equal to the outer diameters of the firstand second ends of the first section, wherein said frictional engagementof said first means for joining is between said inner diameter of saidhollow inner portion at said distal end and said outer diameter of saidsecond end, and said frictional engagement of said second means forjoining is between said inner diameter of said hollow inner portion atsaid proximal end and said outer diameter of said first end.
 26. The kitfor an annuloplasty ring of claim 23, wherein the distal end of thesecond flexible section further comprises a hollow inner portion with aninner diameter approximately equal to the outer diameter of theattaching end of the needle and said frictional engagement of said meansfor joining the distal end to a needle is between said inner diameterand said outer diameter of the attaching end.
 27. The kit for anannuloplasty ring of claim 21, wherein said second flexible sectionfurther comprising a means for sizing the ring.
 28. An annuloplasty ringfor use in an annuloplasty surgical procedure to correct mitralinsufficiency in a patient by restoring the mitral valve annulus to anormal shape and flexibility which is determined by the movement of theleft ventricle, the mitral valve and the mitral valve annulus, whereinsaid annuloplasty ring comprises: a first rigid section having a firstend, a second end and a length, said first and second ends having anouter diameter; a second flexible section having a distal end, aproximal end, a length, a means for sizing the ring, and at least onehollow inner portion with an exterior opening at the proximal and distalends and an inner diameter; a round-tip needle having a tip and anattaching end with an outer diameter; a first means for joining thedistal end of the second section to the second end of the first section;a second means for joining the proximal end of the second section to thefirst end of the first section; a third means for joining the distal endof the second section to the needle; wherein said outer diameters of thefirst section and the outer diameter of the attaching end areapproximately equal to the inner diameter of the hollow inner portionand said length of said second flexible section is greater than saidlength of said first rigid section; said first means for joiningcomprising a frictional engagement between the inner diameter of thehollow inner portion at the distal end and the outer diameter of thesecond end; said second means for joining comprising a frictionalengagement between the inner diameter of the hollow inner portion at theproximal end and the outer diameter of the first end; and said thirdmeans for joining comprising a frictional engagement between the innerdiameter of the hollow inner portion at the distal end and the outerdiameter of the attaching end of the needle; said means for sizing thering further comprising measurement indicia on the distal end of thesecond section; said first rigid section is substantially straight andfurther comprises a bow positioned between the first and second ends;the annuloplasty ring further comprising: (1) an open configurationdefined by said first section being joined to said second section bysaid second means for joining, wherein the exterior opening and hollowinner portion at the proximal end of the second section receive thefirst end of the first section therein, the first end and the proximalend are held together by said frictional engagement, and said second endand said distal end being unattached; (2) a surgical configurationdefined by said first section being joined to said second section andsaid needle by said second and third means for joining, wherein saidexterior opening and hollow inner portion at the proximal end of thesecond section receive the first end of said first section therein, thefirst end and proximal end are held together by said frictionalengagement of said second means for joining and said distal end of saidsecond section, and the exterior opening and hollow inner portion at thedistal end of the second section receive the attaching end of the needletherein, the distal end and the attaching end are held together by saidfrictional engagement of the third means for joining; and (3) a closedconfiguration defined by said first section being joined to said secondsection by said first and second means for joining, wherein the exterioropening and the hollow inner portion at the proximal end of said secondsection receive the first end of said first section therein, theproximal end and the first end are held by said frictional engagement ofsaid second means for joining, and said exterior opening and the hollowinner portion at the distal end of the second section receive the secondend of the first section therein, the distal end and the second end areheld by said frictional engagement of said first means for joining;wherein said first rigid section for implantation adjacent to ananterior portion of the mitral valve annulus and said second section forimplantation in the fat pad of the atrioventricular groove.
 29. A methodfor implanting an annuloplasty ring in a patient's heart to correctmitral insufficiency in which the mitral valve annulus is restored to anormal shape and flexibility as determined by the movement of the leftventricle, the mitral valve and the mitral valve annulus, the stepscomprising: (1) providing an annuloplasty ring having an elongatedflexible section attached at one end to a rigid section with a bow andattached at an opposite end to a round tipped-needle; (2) inserting thetip of the needle through the endocardium and the left atrial myocardialwall of the heart from the endocardial aspect, at the right fibroustrigone; (3) passing the needle and a portion of the annuloplasty ringthrough the endocardium and the left atrial myocardial wall of the heartfrom the endocardial aspect, at the right fibrous trigone; (4) passingthe needle and a portion of the annuloplasty ring in a posteriordirection just external to and parallel to the mitral valve annulus; (5)passing the needle and a portion of the annuloplasty ring around theoutside of the mitral valve annulus in the fat pad of theatrioventricular groove in a clockwise direction to the left fibroustrigone; (6) inserting the tip of the needle back through the leftatrial myocardial wall and the endocardium from the epicardial aspect atthe left fibrous trigone; (7) passing the needle and a portion of theannuloplasty ring back through the left atrial myocardial wall from theepicardial aspect and back through the endocardium at the left fibroustrigone; (8) positioning the flexible section substantially parallel toa posterior portion of the mitral valve annulus; (9) aligning the rigidsection along an anterior portion of the mitral valve annulus, (10)positioning the bow of the rigid section conforms to a contour of themitral valve annulus adjacent the aortic valve root and furtherpositioning the flexible section around a posterior portion of themitral vale annulus; (11) detaching the needle from the flexiblesection; (12) determining the appropriate size of the annuloplasty ring;(13) cutting the flexible section of the annuloplasty to the appropriatesize; (14) closing the annuloplasty ring by affixing the distal end ofthe flexible section to the second end of the rigid section by insertingthe rigid section into the inner hollow portion of the flexible section;(15) suturing the annuloplasty ring to valve annulus which at the leftand right fibrous trigones; (16) suturing one point along the posteriorsection of the mitral valve annulus to the flexible section of theannuloplasty ring.
 30. A kit for an annuloplasty ring to be used in anannuloplasty surgical procedure to correct mitral insufficiency in apatient by restoring the mitral valve annulus to a normal shape andflexibility which is determined by the movement of the left ventricle,the mitral valve and the mitral valve annulus, wherein said annuloplastyring comprises: a first rigid section having a first end, a second end,a length and an outer diameter; a second flexible section having adistal end, a proximal end, a length, a means for sizing the ring, andat least one hollow inner portion with an exterior opening at the distaland proximal ends and an inner diameter; a round-tip needle having a tipand an attaching end with an outer diameter; a first means for joiningthe distal end of the second section to the second end of the firstsection; a second means for joining the proximal end of the secondsection to the first end of the first section; a third means for joiningthe distal end of the second section to the needle; wherein said outerdiameter of the first section and the outer diameter of the attachingend are approximately equal to the inner diameter of the hollow innerportion; said first means for joining comprising a frictional engagementbetween the inner diameter of the hollow inner portion at the distal endand the outer diameter of the second end when the two ends are joined;said second means for joining comprising a frictional engagement betweenthe inner diameter of the hollow inner portion at the proximal end andthe outer diameter of the first end when the two ends are joined; andsaid third means for joining comprising a frictional engagement betweenthe inner diameter of the hollow inner portion at the distal end and theouter diameter of the attaching end of the needle when the two ends arejoined.